|
autosomal recessive deafness 48
|
12273 |
|
|
autosomal recessive nonsyndromic deafness 48
|
12273 |
|
|
autosomal recessive nonsyndromic deafness caused by mutation in CIB2
|
12273 |
|
|
autosomal recessive nonsyndromic deafness type 48
|
12273 |
|
|
choroideraemia co-occurrent with hypopituitarism
|
22737 |
|
|
choroideremia co-occurrent with hypopituitarism
|
22737 |
|
|
deafness, autosomal recessive 48
|
12273 |
|
|
deafness, autosomal recessive 48; DFNB48
|
http://purl.obolibrary.org/obo/MONDO_0012273 |
|
|
CIB2 autosomal recessive nonsyndromic deafness
|
12273 |
|
|
deafness, autosomal recessive type 48
|
12273 |
|
